CA2406230A1 - Dispersants - Google Patents
Dispersants Download PDFInfo
- Publication number
- CA2406230A1 CA2406230A1 CA002406230A CA2406230A CA2406230A1 CA 2406230 A1 CA2406230 A1 CA 2406230A1 CA 002406230 A CA002406230 A CA 002406230A CA 2406230 A CA2406230 A CA 2406230A CA 2406230 A1 CA2406230 A1 CA 2406230A1
- Authority
- CA
- Canada
- Prior art keywords
- acid
- dispersant
- formula
- poac
- group
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 239000002270 dispersing agent Substances 0.000 title claims abstract description 171
- 239000002253 acid Substances 0.000 claims abstract description 112
- -1 phosphate ester Chemical class 0.000 claims abstract description 35
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 33
- 150000002596 lactones Chemical class 0.000 claims abstract description 26
- 229910019142 PO4 Inorganic materials 0.000 claims abstract description 15
- 239000010452 phosphate Substances 0.000 claims abstract description 15
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims abstract description 11
- 150000001875 compounds Chemical class 0.000 claims description 52
- 239000007787 solid Substances 0.000 claims description 43
- 239000000203 mixture Substances 0.000 claims description 38
- 229920000083 poly(allylamine) Polymers 0.000 claims description 25
- 125000000217 alkyl group Chemical group 0.000 claims description 24
- 239000003795 chemical substances by application Substances 0.000 claims description 24
- 239000006185 dispersion Substances 0.000 claims description 24
- 150000003839 salts Chemical class 0.000 claims description 19
- PAPBSGBWRJIAAV-UHFFFAOYSA-N ε-Caprolactone Chemical compound O=C1CCCCCO1 PAPBSGBWRJIAAV-UHFFFAOYSA-N 0.000 claims description 19
- 229920005989 resin Polymers 0.000 claims description 17
- 239000011347 resin Substances 0.000 claims description 17
- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 claims description 16
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 16
- 125000001931 aliphatic group Chemical group 0.000 claims description 15
- WNWHHMBRJJOGFJ-UHFFFAOYSA-N 16-methylheptadecan-1-ol Chemical compound CC(C)CCCCCCCCCCCCCCCO WNWHHMBRJJOGFJ-UHFFFAOYSA-N 0.000 claims description 12
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 claims description 12
- 125000004432 carbon atom Chemical group C* 0.000 claims description 12
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 11
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims description 11
- 229940117927 ethylene oxide Drugs 0.000 claims description 11
- 239000003973 paint Substances 0.000 claims description 11
- 239000004721 Polyphenylene oxide Chemical group 0.000 claims description 9
- 150000001408 amides Chemical class 0.000 claims description 9
- 238000000034 method Methods 0.000 claims description 9
- 229920000570 polyether Chemical group 0.000 claims description 9
- 229940114072 12-hydroxystearic acid Drugs 0.000 claims description 8
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 claims description 8
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 230000008569 process Effects 0.000 claims description 8
- 239000012298 atmosphere Substances 0.000 claims description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 7
- JMOLZNNXZPAGBH-UHFFFAOYSA-N hexyldecanoic acid Chemical compound CCCCCCCCC(C(O)=O)CCCCCC JMOLZNNXZPAGBH-UHFFFAOYSA-N 0.000 claims description 7
- 239000001301 oxygen Substances 0.000 claims description 7
- 229910021653 sulphate ion Inorganic materials 0.000 claims description 7
- PRNCMAKCNVRZFX-UHFFFAOYSA-N 3,7-dimethyloctan-1-ol Chemical compound CC(C)CCCC(C)CCO PRNCMAKCNVRZFX-UHFFFAOYSA-N 0.000 claims description 6
- RZKSECIXORKHQS-UHFFFAOYSA-N Heptan-3-ol Chemical compound CCCCC(O)CC RZKSECIXORKHQS-UHFFFAOYSA-N 0.000 claims description 6
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 6
- 125000003118 aryl group Chemical group 0.000 claims description 6
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 claims description 6
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 claims description 6
- 229960003656 ricinoleic acid Drugs 0.000 claims description 6
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 claims description 6
- DNIAPMSPPWPWGF-GSVOUGTGSA-N (R)-(-)-Propylene glycol Chemical compound C[C@@H](O)CO DNIAPMSPPWPWGF-GSVOUGTGSA-N 0.000 claims description 5
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 5
- ZDHCZVWCTKTBRY-UHFFFAOYSA-N 12-hydroxylauric acid Chemical compound OCCCCCCCCCCCC(O)=O ZDHCZVWCTKTBRY-UHFFFAOYSA-N 0.000 claims description 4
- OYXVDHZABMXCMX-UHFFFAOYSA-N 2-decyltetradecanoic acid Chemical compound CCCCCCCCCCCCC(C(O)=O)CCCCCCCCCC OYXVDHZABMXCMX-UHFFFAOYSA-N 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 4
- TZYRSLHNPKPEFV-UHFFFAOYSA-N 2-ethyl-1-butanol Chemical compound CCC(CC)CO TZYRSLHNPKPEFV-UHFFFAOYSA-N 0.000 claims description 3
- KUIYXYIWGVFQPD-UHFFFAOYSA-N 2-octyldodecanoic acid Chemical compound CCCCCCCCCCC(C(O)=O)CCCCCCCC KUIYXYIWGVFQPD-UHFFFAOYSA-N 0.000 claims description 3
- BODRLKRKPXBDBN-UHFFFAOYSA-N 3,5,5-Trimethyl-1-hexanol Chemical compound OCCC(C)CC(C)(C)C BODRLKRKPXBDBN-UHFFFAOYSA-N 0.000 claims description 3
- 239000012442 inert solvent Substances 0.000 claims description 3
- OBETXYAYXDNJHR-SSDOTTSWSA-M (2r)-2-ethylhexanoate Chemical compound CCCC[C@@H](CC)C([O-])=O OBETXYAYXDNJHR-SSDOTTSWSA-M 0.000 claims description 2
- LMHJFKYQYDSOQO-SECBINFHSA-N (5r)-5-hydroxydecanoic acid Chemical compound CCCCC[C@@H](O)CCCC(O)=O LMHJFKYQYDSOQO-SECBINFHSA-N 0.000 claims description 2
- OXQGTIUCKGYOAA-UHFFFAOYSA-N 2-Ethylbutanoic acid Chemical compound CCC(CC)C(O)=O OXQGTIUCKGYOAA-UHFFFAOYSA-N 0.000 claims description 2
- NYHNVHGFPZAZGA-UHFFFAOYSA-N 2-hydroxyhexanoic acid Chemical compound CCCCC(O)C(O)=O NYHNVHGFPZAZGA-UHFFFAOYSA-N 0.000 claims description 2
- QQAVZEYXLCYOKO-UHFFFAOYSA-N 4-Hydroxycapric acid Chemical compound CCCCCCC(O)CCC(O)=O QQAVZEYXLCYOKO-UHFFFAOYSA-N 0.000 claims description 2
- VEZXCJBBBCKRPI-UHFFFAOYSA-N beta-propiolactone Chemical compound O=C1CCO1 VEZXCJBBBCKRPI-UHFFFAOYSA-N 0.000 claims description 2
- 150000001768 cations Chemical class 0.000 claims description 2
- LMHJFKYQYDSOQO-UHFFFAOYSA-N hydroxydecanoic acid Natural products CCCCCC(O)CCCC(O)=O LMHJFKYQYDSOQO-UHFFFAOYSA-N 0.000 claims description 2
- LXNOENXQFNYMGT-UHFFFAOYSA-N xi-5-Hydroxydodecanoic acid Chemical compound CCCCCCCC(O)CCCC(O)=O LXNOENXQFNYMGT-UHFFFAOYSA-N 0.000 claims description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 2
- OZJPLYNZGCXSJM-UHFFFAOYSA-N 5-valerolactone Chemical class O=C1CCCCO1 OZJPLYNZGCXSJM-UHFFFAOYSA-N 0.000 claims 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 claims 2
- HPDXGZJYWFFBGM-UHFFFAOYSA-N 2-butyloctanoic acid Chemical compound CCCCCCC(C(O)=O)CCCC.CCCCCCC(C(O)=O)CCCC HPDXGZJYWFFBGM-UHFFFAOYSA-N 0.000 claims 1
- YJKUIGNKIIFRAL-UHFFFAOYSA-N 2-hydroxypentanoic acid;2-hydroxypropanoic acid Chemical compound CC(O)C(O)=O.CCCC(O)C(O)=O YJKUIGNKIIFRAL-UHFFFAOYSA-N 0.000 claims 1
- 229920002873 Polyethylenimine Polymers 0.000 abstract description 52
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 14
- 229920000768 polyamine Polymers 0.000 abstract description 11
- 150000001298 alcohols Chemical class 0.000 abstract description 9
- 125000002843 carboxylic acid group Chemical group 0.000 abstract description 9
- 150000007513 acids Chemical class 0.000 abstract description 8
- 125000000129 anionic group Chemical group 0.000 abstract 1
- 150000001412 amines Chemical class 0.000 description 35
- 241000640882 Condea Species 0.000 description 33
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 31
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 30
- 238000006243 chemical reaction Methods 0.000 description 27
- 230000002378 acidificating effect Effects 0.000 description 26
- 239000007788 liquid Substances 0.000 description 22
- 239000000543 intermediate Substances 0.000 description 20
- 229910052757 nitrogen Inorganic materials 0.000 description 19
- 239000000047 product Substances 0.000 description 16
- 239000000376 reactant Substances 0.000 description 15
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 12
- 239000002585 base Substances 0.000 description 12
- 239000000049 pigment Substances 0.000 description 11
- 229920000728 polyester Polymers 0.000 description 11
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 10
- 239000000976 ink Substances 0.000 description 10
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 9
- 229920000137 polyphosphoric acid Polymers 0.000 description 9
- 239000002904 solvent Substances 0.000 description 9
- XMVBHZBLHNOQON-UHFFFAOYSA-N 2-butyl-1-octanol Chemical compound CCCCCCC(CO)CCCC XMVBHZBLHNOQON-UHFFFAOYSA-N 0.000 description 8
- ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 description 8
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 8
- 238000001816 cooling Methods 0.000 description 8
- LEACJMVNYZDSKR-UHFFFAOYSA-N 2-octyldodecan-1-ol Chemical compound CCCCCCCCCCC(CO)CCCCCCCC LEACJMVNYZDSKR-UHFFFAOYSA-N 0.000 description 7
- CCTFMNIEFHGTDU-UHFFFAOYSA-N 3-methoxypropyl acetate Chemical compound COCCCOC(C)=O CCTFMNIEFHGTDU-UHFFFAOYSA-N 0.000 description 7
- DHMQDGOQFOQNFH-UHFFFAOYSA-N Glycine Chemical compound NCC(O)=O DHMQDGOQFOQNFH-UHFFFAOYSA-N 0.000 description 7
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 7
- 239000003054 catalyst Substances 0.000 description 7
- 238000003801 milling Methods 0.000 description 7
- 239000003921 oil Substances 0.000 description 7
- 235000019198 oils Nutrition 0.000 description 7
- 229910052698 phosphorus Inorganic materials 0.000 description 7
- 239000002243 precursor Substances 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- XULHFMYCBKQGEE-UHFFFAOYSA-N 2-hexyl-1-Decanol Chemical compound CCCCCCCCC(CO)CCCCCC XULHFMYCBKQGEE-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 6
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 6
- MWKFXSUHUHTGQN-UHFFFAOYSA-N decan-1-ol Chemical compound CCCCCCCCCCO MWKFXSUHUHTGQN-UHFFFAOYSA-N 0.000 description 6
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 6
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 description 6
- 238000005886 esterification reaction Methods 0.000 description 6
- 229950004531 hexyldecanoic acid Drugs 0.000 description 6
- 239000012948 isocyanate Substances 0.000 description 6
- XULHFMYCBKQGEE-MRXNPFEDSA-N 2-Hexyl-1-decanol Natural products CCCCCCCC[C@H](CO)CCCCCC XULHFMYCBKQGEE-MRXNPFEDSA-N 0.000 description 5
- OARDBPIZDHVTCK-UHFFFAOYSA-N 2-butyloctanoic acid Chemical compound CCCCCCC(C(O)=O)CCCC OARDBPIZDHVTCK-UHFFFAOYSA-N 0.000 description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 5
- 150000002009 diols Chemical class 0.000 description 5
- 230000032050 esterification Effects 0.000 description 5
- 150000002466 imines Chemical class 0.000 description 5
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 5
- 239000001117 sulphuric acid Substances 0.000 description 5
- 235000011149 sulphuric acid Nutrition 0.000 description 5
- 229910052720 vanadium Inorganic materials 0.000 description 5
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- DKPFZGUDAPQIHT-UHFFFAOYSA-N Butyl acetate Natural products CCCCOC(C)=O DKPFZGUDAPQIHT-UHFFFAOYSA-N 0.000 description 4
- QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 description 4
- AVXURJPOCDRRFD-UHFFFAOYSA-N Hydroxylamine Chemical compound ON AVXURJPOCDRRFD-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- 102100035593 POU domain, class 2, transcription factor 1 Human genes 0.000 description 4
- 101710084414 POU domain, class 2, transcription factor 1 Proteins 0.000 description 4
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 4
- 125000002947 alkylene group Chemical group 0.000 description 4
- 125000003277 amino group Chemical group 0.000 description 4
- BSDOQSMQCZQLDV-UHFFFAOYSA-N butan-1-olate;zirconium(4+) Chemical compound [Zr+4].CCCC[O-].CCCC[O-].CCCC[O-].CCCC[O-] BSDOQSMQCZQLDV-UHFFFAOYSA-N 0.000 description 4
- 229940043232 butyl acetate Drugs 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- RBTKNAXYKSUFRK-UHFFFAOYSA-N heliogen blue Chemical compound [Cu].[N-]1C2=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=NC([N-]1)=C(C=CC=C3)C3=C1N=C([N-]1)C3=CC=CC=C3C1=N2 RBTKNAXYKSUFRK-UHFFFAOYSA-N 0.000 description 4
- FUZZWVXGSFPDMH-UHFFFAOYSA-N hexanoic acid Chemical compound CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 description 4
- 229910052739 hydrogen Inorganic materials 0.000 description 4
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 4
- 239000013067 intermediate product Substances 0.000 description 4
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 4
- 239000000314 lubricant Substances 0.000 description 4
- 150000007524 organic acids Chemical class 0.000 description 4
- 239000012860 organic pigment Substances 0.000 description 4
- 239000011574 phosphorus Substances 0.000 description 4
- 239000004033 plastic Substances 0.000 description 4
- 229920003023 plastic Polymers 0.000 description 4
- 229920005862 polyol Polymers 0.000 description 4
- 150000003077 polyols Chemical class 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- FYSNRJHAOHDILO-UHFFFAOYSA-N thionyl chloride Chemical compound ClS(Cl)=O FYSNRJHAOHDILO-UHFFFAOYSA-N 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
- TXWSZJSDZKWQAU-UHFFFAOYSA-N 2,9-dimethyl-5,12-dihydroquinolino[2,3-b]acridine-7,14-dione Chemical compound N1C2=CC=C(C)C=C2C(=O)C2=C1C=C(C(=O)C=1C(=CC=C(C=1)C)N1)C1=C2 TXWSZJSDZKWQAU-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 239000004606 Fillers/Extenders Substances 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 239000004471 Glycine Substances 0.000 description 3
- 239000005639 Lauric acid Substances 0.000 description 3
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 3
- 229920000877 Melamine resin Polymers 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 description 3
- 125000004450 alkenylene group Chemical group 0.000 description 3
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 3
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexyloxide Natural products O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 3
- 150000002170 ethers Chemical class 0.000 description 3
- 229940093476 ethylene glycol Drugs 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- IVJISJACKSSFGE-UHFFFAOYSA-N formaldehyde;1,3,5-triazine-2,4,6-triamine Chemical compound O=C.NC1=NC(N)=NC(N)=N1 IVJISJACKSSFGE-UHFFFAOYSA-N 0.000 description 3
- 150000002334 glycols Chemical class 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 125000001841 imino group Chemical group [H]N=* 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- UEZVMMHDMIWARA-UHFFFAOYSA-M phosphonate Chemical compound [O-]P(=O)=O UEZVMMHDMIWARA-UHFFFAOYSA-M 0.000 description 3
- 235000011007 phosphoric acid Nutrition 0.000 description 3
- 125000004437 phosphorous atom Chemical group 0.000 description 3
- 239000001054 red pigment Substances 0.000 description 3
- 125000001302 tertiary amino group Chemical group 0.000 description 3
- 238000010792 warming Methods 0.000 description 3
- 229940045860 white wax Drugs 0.000 description 3
- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- HXVNBWAKAOHACI-UHFFFAOYSA-N 2,4-dimethyl-3-pentanone Chemical compound CC(C)C(=O)C(C)C HXVNBWAKAOHACI-UHFFFAOYSA-N 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- LTHNHFOGQMKPOV-UHFFFAOYSA-N 2-ethylhexan-1-amine Chemical compound CCCCC(CC)CN LTHNHFOGQMKPOV-UHFFFAOYSA-N 0.000 description 2
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- 150000003751 zinc Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000004246 zinc acetate Substances 0.000 description 1
- 239000011787 zinc oxide Substances 0.000 description 1
- 150000003754 zirconium Chemical class 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D17/00—Pigment pastes, e.g. for mixing in paints
- C09D17/002—Pigment pastes, e.g. for mixing in paints in organic medium
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0071—Process features in the making of dyestuff preparations; Dehydrating agents; Dispersing agents; Dustfree compositions
- C09B67/0084—Dispersions of dyes
- C09B67/0085—Non common dispersing agents
- C09B67/0089—Non common dispersing agents non ionic dispersing agent, e.g. EO or PO addition products
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D11/00—Inks
- C09D11/02—Printing inks
- C09D11/03—Printing inks characterised by features other than the chemical nature of the binder
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C09D167/06—Unsaturated polyesters having carbon-to-carbon unsaturation
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
- C09D7/40—Additives
- C09D7/45—Anti-settling agents
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/14—Derivatives of phosphoric acid
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/16—Amines or polyamines
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
- C09K23/18—Quaternary ammonium compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Dispersion Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Lubricants (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Polyesters Or Polycarbonates (AREA)
Abstract
L'invention concerne des dispersants acides et basiques, dérivés d'acides et d'alcools aliphatiques d'alkyle ramifié ainsi que d'acide ou de lactone hydroxy-carboxylique pour donner une chaîne polyoxyalkylènecarbonyle (POAC), présentant un groupe d'acides carboxyliques terminaux (acide TPOAC) ou un groupe hydroxy terminal (alcool TPOAC). On obtient des dispersants basiques préférés, en réunissant un ou plusieurs acides TPOAC avec une polyamine ou polyimine, telle qu'une polyéthylèneimine, et on prépare des dispersants anioniques préférés, en produisant un ester phosphorique d'un alcool TPOAC.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0009798.0A GB0009798D0 (en) | 2000-04-20 | 2000-04-20 | Dispersants |
GB0009798.0 | 2000-04-20 | ||
PCT/GB2001/001524 WO2001080987A2 (fr) | 2000-04-20 | 2001-04-04 | Dispersants |
Publications (1)
Publication Number | Publication Date |
---|---|
CA2406230A1 true CA2406230A1 (fr) | 2001-11-01 |
Family
ID=9890310
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA002406230A Abandoned CA2406230A1 (fr) | 2000-04-20 | 2001-04-04 | Dispersants |
Country Status (14)
Country | Link |
---|---|
US (1) | US7348367B2 (fr) |
EP (2) | EP1702672B1 (fr) |
JP (1) | JP4874490B2 (fr) |
KR (1) | KR100711642B1 (fr) |
CN (3) | CN1437504B (fr) |
AT (2) | ATE400355T1 (fr) |
AU (1) | AU2001244388A1 (fr) |
BR (1) | BR0110199A (fr) |
CA (1) | CA2406230A1 (fr) |
DE (1) | DE60134733D1 (fr) |
ES (1) | ES2309057T3 (fr) |
GB (1) | GB0009798D0 (fr) |
MX (1) | MXPA02010257A (fr) |
WO (1) | WO2001080987A2 (fr) |
Families Citing this family (46)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB0109708D0 (en) * | 2001-04-20 | 2001-06-13 | Avecia Ltd | Dispersants |
GB0311121D0 (en) | 2003-05-15 | 2003-06-18 | Avecia Ltd | Polyurethane dispersants |
JP4407175B2 (ja) * | 2003-06-30 | 2010-02-03 | 東洋インキ製造株式会社 | 顔料分散体およびその使用 |
GB0316857D0 (en) * | 2003-07-18 | 2003-08-20 | Avecia Ltd | Compositions |
US7872070B2 (en) * | 2004-12-21 | 2011-01-18 | Lubrizol Limited | Compositions |
DE602005016018D1 (de) * | 2004-12-21 | 2009-09-24 | Lubrizol Ltd | Zusammensetzungen |
DE602005017304D1 (de) * | 2004-12-23 | 2009-12-03 | Lubrizol Ltd | Dispersionsmittel |
DE102005004024A1 (de) * | 2005-01-28 | 2006-08-03 | Goldschmidt Gmbh | Polyether/Polyester enthaltende Dispergierharze |
US8772435B2 (en) * | 2005-04-13 | 2014-07-08 | Lubrizol Advanced Materials, Inc. | Dispersants |
EP1879689B1 (fr) * | 2005-05-12 | 2014-07-09 | Lubrizol Limited | Dispersants et compositions les contenant |
DE102005055711A1 (de) * | 2005-11-23 | 2007-05-24 | Degussa Gmbh | Feststoffe/Polyether/Polyester enthaltende Dispergiermittel |
EP1999185B1 (fr) * | 2006-03-29 | 2012-02-29 | Basf Se | Dispersants de pigments a base de polyethylene imine |
DE602006015324D1 (de) * | 2006-10-11 | 2010-08-19 | Agfa Graphics Nv | Pigmentierte nicht wässrige Tinte für Tintenstrahldrucker |
ATE440127T1 (de) * | 2006-10-11 | 2009-09-15 | Agfa Graphics Nv | Nichtwässrige, pigmentierte tintenstrahldruckfarbe |
EP1911813B1 (fr) * | 2006-10-11 | 2009-08-19 | Agfa Graphics N.V. | Encre a jet d'encre non-aqueuse et pigmentée |
US7923474B2 (en) * | 2007-02-27 | 2011-04-12 | Ppg Industries Ohio, Inc. | Amine dispersants, organic dispersions and related coating compositions |
ATE540062T1 (de) * | 2007-03-05 | 2012-01-15 | Basf Se | Polyamin-polyacrylat-dispergiermittel |
TW200904518A (en) * | 2007-03-28 | 2009-02-01 | Lubrizol Ltd | Dispersant composition |
TW200904517A (en) * | 2007-03-28 | 2009-02-01 | Lubrizol Ltd | Dispersant composition |
US20100204435A1 (en) * | 2007-09-04 | 2010-08-12 | Keio University | 12-hydroxstearic acid copolymer and method for producing the same |
BRPI0918664A2 (pt) * | 2008-09-18 | 2015-12-01 | Lubrizol Advanced Mat Inc | composição, produto, processo para preparar o composto, e, uso do composto |
AU2010340940B2 (en) * | 2009-12-17 | 2013-09-19 | Basf Se | Aqueous coating formulation |
IT1404805B1 (it) | 2011-02-10 | 2013-11-29 | Lamberti Spa | Disperdenti |
ITVA20110006A1 (it) * | 2011-03-03 | 2012-09-04 | Lamberti Spa | Inchiostri ceramici per stampanti inkjet |
US8815484B2 (en) | 2011-10-12 | 2014-08-26 | Canon Kabushiki Kaisha | Toner including compound having bisazo skeleton |
WO2013054938A1 (fr) | 2011-10-12 | 2013-04-18 | Canon Kabushiki Kaisha | Composé ayant un squelette bisazo, dispersant de pigment contenant le composé, composition de pigment, dispersion de pigment, encre et composition de réserve pour un filtre coloré |
JP5936106B2 (ja) * | 2011-11-25 | 2016-06-15 | 第一工業製薬株式会社 | 金属酸化物半導体粒子分散体組成物および半導体の製造方法 |
EP2634633B1 (fr) | 2012-02-29 | 2015-07-01 | Canon Kabushiki Kaisha | Toner cyan contenant un composé ayant un squelette azo |
EP2634632A1 (fr) | 2012-02-29 | 2013-09-04 | Canon Kabushiki Kaisha | Toner noir contenant un composé ayant un squelette azo |
CN103881103A (zh) * | 2012-12-21 | 2014-06-25 | 上海飞凯光电材料股份有限公司 | 一种超分散剂的合成方法及应用 |
US9625845B2 (en) | 2013-04-30 | 2017-04-18 | Canon Kabushiki Kaisha | Compound having azo skeleton structure, pigment-dispersing agent, pigment composition, pigment dispersion, and toner |
US9593243B2 (en) | 2013-08-28 | 2017-03-14 | Canon Kabushiki Kaisha | Compound, pigment dispersing agent, pigment composition, pigment dispersion and toner containing said compound |
US10087328B2 (en) | 2013-08-29 | 2018-10-02 | Canon Kabushiki Kaisha | Compound having azo skeleton, pigment dispersant, pigment composition, pigment dispersion, and toner |
EP3063239A1 (fr) | 2013-11-01 | 2016-09-07 | Lubrizol Advanced Materials, Inc. | Dispersants comportant de multiples groupes d'ancrage à base d'imides aromatiques |
CN103753503A (zh) * | 2013-12-23 | 2014-04-30 | 惠州柯林电器有限公司 | 橡胶钉拆卸器 |
EP3233260B1 (fr) * | 2014-12-19 | 2019-08-28 | Nouryon Chemicals International B.V. | Dispersant universel |
US9618867B2 (en) | 2015-02-20 | 2017-04-11 | Canon Kabushiki Kaisha | Pigment dispersion and toner |
BR112018014742B1 (pt) * | 2016-01-22 | 2022-09-20 | Basf Se | Composições de dispersante e aquosa de pigmento, e, usos de uma composição dispersante e aquosa de pigmento |
EP3222650A1 (fr) * | 2016-03-24 | 2017-09-27 | Evonik Degussa GmbH | Agent de dispersion |
CN111229117B (zh) * | 2018-11-29 | 2022-01-04 | 中国石油化工股份有限公司 | 含脂肪酸型表面活性剂的混合体系及其制备方法 |
CN111229120B (zh) * | 2018-11-29 | 2022-01-07 | 中国石油化工股份有限公司 | 含脂肪酸型表面活性剂的混合体系及其制备方法 |
TW202045248A (zh) * | 2019-03-14 | 2020-12-16 | 美商盧伯利索先進材料有限公司 | 經由酸酐中間物製得之多胺分散劑 |
JP6799288B1 (ja) | 2019-12-20 | 2020-12-16 | 東洋インキScホールディングス株式会社 | 活性エネルギー線硬化型インクジェットインキ、及び、活性エネルギー線硬化型インキセット |
CN111690134A (zh) * | 2020-07-03 | 2020-09-22 | 江苏道赢科技有限公司 | 一种提升阴极片软韧性的分散剂 |
EP4101874A1 (fr) | 2021-06-08 | 2022-12-14 | Evonik Operations GmbH | Dispersants de polyamidoamine |
PL3943526T3 (pl) | 2020-07-23 | 2024-05-20 | Evonik Operations Gmbh | Dyspergatory poliamidoaminowe |
Family Cites Families (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3704255A (en) * | 1971-03-03 | 1972-11-28 | Du Pont | Polyesters |
GB8402801D0 (en) * | 1984-02-02 | 1984-03-07 | Ici Plc | Dispersion |
EP0164817B1 (fr) | 1984-03-21 | 1991-01-23 | Imperial Chemical Industries Plc | Détergent |
EP0208041B1 (fr) * | 1985-01-22 | 1991-05-15 | Imperial Chemical Industries Plc | Composition contenant un dispersant |
US5011629A (en) * | 1989-04-17 | 1991-04-30 | Bilbo Raymond E | Hydroxystearic polyesters of guerbet alcohols as polycarbonate lubricants |
DE3930687A1 (de) * | 1989-09-14 | 1991-04-11 | Byk Chemie Gmbh | Phosphorsaeureester, verfahren zu deren herstellung und deren verwendung als dispergiermittel |
DE3934882A1 (de) † | 1989-10-19 | 1991-04-25 | Gruenau Gmbh Chem Fab | Waessrige, carbonsaeuren und/oder harzsaeuren enthaltende dispersionen zum deinken von bedruckten altpapieren |
JPH0611390B2 (ja) * | 1990-04-20 | 1994-02-16 | 第一工業製薬株式会社 | 微粉末の非水系分散剤 |
GB9100614D0 (en) | 1991-01-11 | 1991-02-27 | Xaar Ltd | Ink composition |
GB9306222D0 (en) | 1993-03-25 | 1993-05-19 | Zeneca Ltd | Dispersants |
JPH0810601A (ja) * | 1994-06-27 | 1996-01-16 | Daicel Chem Ind Ltd | 顔料分散剤およびラクトン変性アミン化合物の製造方法 |
JP3313897B2 (ja) * | 1994-08-01 | 2002-08-12 | ダイセル化学工業株式会社 | 顔料分散剤 |
US6194539B1 (en) † | 1994-11-22 | 2001-02-27 | Daicel Chemical Industries, Inc. | Polylactone having amino groups, a process for the preparation thereof, a compound having amino group, a composition for coatings, a composition for printing inks |
CA2178663A1 (fr) * | 1995-07-06 | 1997-01-07 | Richard E. Cherpeck | Aminocarbamates de polylactones et compositions combustibles qui en renferment |
GB9622783D0 (en) * | 1996-11-01 | 1997-01-08 | Zeneca Ltd | Dispersants |
JP3625351B2 (ja) * | 1997-02-25 | 2005-03-02 | 竹本油脂株式会社 | 合成繊維用潤滑剤及び合成繊維処理方法 |
GB9806723D0 (en) | 1998-03-28 | 1998-05-27 | Zeneca Ltd | Dispersants |
GB9809025D0 (en) * | 1998-04-28 | 1998-06-24 | Zeneca Ltd | Amine dispersants |
GB9809116D0 (en) † | 1998-04-29 | 1998-07-01 | Zeneca Ltd | Ether/ester dispersants |
GB9922039D0 (en) * | 1999-09-18 | 1999-11-17 | Avecia Ltd | Polyester dispersants |
-
2000
- 2000-04-20 GB GBGB0009798.0A patent/GB0009798D0/en not_active Ceased
-
2001
- 2001-04-04 CN CN018114415A patent/CN1437504B/zh not_active Expired - Fee Related
- 2001-04-04 CN CNA2006100591539A patent/CN1846833A/zh active Pending
- 2001-04-04 WO PCT/GB2001/001524 patent/WO2001080987A2/fr active IP Right Grant
- 2001-04-04 AU AU2001244388A patent/AU2001244388A1/en not_active Abandoned
- 2001-04-04 AT AT01917307T patent/ATE400355T1/de not_active IP Right Cessation
- 2001-04-04 ES ES01917307T patent/ES2309057T3/es not_active Expired - Lifetime
- 2001-04-04 MX MXPA02010257A patent/MXPA02010257A/es active IP Right Grant
- 2001-04-04 EP EP06075531A patent/EP1702672B1/fr not_active Expired - Lifetime
- 2001-04-04 US US10/257,132 patent/US7348367B2/en not_active Expired - Lifetime
- 2001-04-04 JP JP2001578077A patent/JP4874490B2/ja not_active Expired - Fee Related
- 2001-04-04 AT AT06075531T patent/ATE444804T1/de not_active IP Right Cessation
- 2001-04-04 DE DE60134733T patent/DE60134733D1/de not_active Expired - Lifetime
- 2001-04-04 CN CN2010102739931A patent/CN101940890B/zh not_active Expired - Fee Related
- 2001-04-04 KR KR1020027014086A patent/KR100711642B1/ko not_active IP Right Cessation
- 2001-04-04 BR BR0110199-4A patent/BR0110199A/pt not_active Application Discontinuation
- 2001-04-04 CA CA002406230A patent/CA2406230A1/fr not_active Abandoned
- 2001-04-04 EP EP01917307A patent/EP1276553B2/fr not_active Expired - Lifetime
Also Published As
Publication number | Publication date |
---|---|
US7348367B2 (en) | 2008-03-25 |
BR0110199A (pt) | 2003-02-04 |
WO2001080987A2 (fr) | 2001-11-01 |
ATE400355T1 (de) | 2008-07-15 |
EP1276553B2 (fr) | 2012-11-07 |
CN1846833A (zh) | 2006-10-18 |
CN1437504A (zh) | 2003-08-20 |
ES2309057T3 (es) | 2008-12-16 |
EP1702672A1 (fr) | 2006-09-20 |
WO2001080987A3 (fr) | 2002-04-25 |
KR100711642B1 (ko) | 2007-04-25 |
EP1276553A2 (fr) | 2003-01-22 |
CN101940890B (zh) | 2013-01-02 |
JP2003531001A (ja) | 2003-10-21 |
EP1702672B1 (fr) | 2009-10-07 |
GB0009798D0 (en) | 2000-06-07 |
US20030181544A1 (en) | 2003-09-25 |
MXPA02010257A (es) | 2003-05-23 |
CN1437504B (zh) | 2011-11-02 |
EP1276553B1 (fr) | 2008-07-09 |
AU2001244388A1 (en) | 2001-11-07 |
KR20030019358A (ko) | 2003-03-06 |
DE60134733D1 (de) | 2008-08-21 |
CN101940890A (zh) | 2011-01-12 |
JP4874490B2 (ja) | 2012-02-15 |
ATE444804T1 (de) | 2009-10-15 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
FZDE | Discontinued |